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Hybrid Clinical Data Management Job at ICON plc, India | Medical Professionals Are Welcome!

Hybrid Clinical Data Management Job at ICON plc

Are you ready to embark on a journey with ICON plc, a leader in healthcare intelligence and clinical research? This hybrid clinical data management job offers a unique opportunity to work at the forefront of the pharmaceutical and biotechnology sectors. Located in Bangalore, Chennai, Trivandrum, and Bengaluru, this role is perfect for professionals with a passion for clinical data and a drive to contribute to innovative treatments and therapies. ICON plc is actively seeking talented individuals to join their dynamic team. If you’re eager to make a significant impact in clinical research, this position might be your next career milestone.

About ICON plc:

ICON plc is a world-leading healthcare intelligence and clinical research organization operating in the pharmaceutical and biotechnology sectors. With a commitment to fostering an inclusive environment, ICON is dedicated to driving innovation and excellence in clinical development. The organization is headquartered in Dublin, Ireland, and has a significant presence in India, where it is actively seeking talent for various roles, including the clinical data management job.

Job Details:

  • Job Title: Clinical Data Coordinator
  • Job Reference: JR156089
  • Location: Bangalore, Chennai, Trivandrum, Bengaluru
  • Job Type: Hybrid
  • Department: ICON Strategic Solutions (FSP)

Clinical Data Management Job Description:

As a Clinical Data Coordinator I at ICON, the selected candidate will design and analyze clinical trials, interpreting complex medical data to contribute to the advancement of innovative treatments and therapies. This hybrid clinical data management job requires a blend of technical expertise and communication skills to ensure the successful delivery of clinical research projects.

Key Responsibilities:

  • Assist the Data Management Study Lead in the development of eCRF, Data Validation Specifications, and Study-Specific Procedures.
  • Review clinical and third-party data based on edit specifications and data review plans.
  • Issue clear, accurate, and concise queries to investigational sites.
  • Communicate effectively with peers, clinical data scientists, and functional management.
  • Perform other project activities to ensure that study timelines are met, including filing and archiving study documentation.

Eligibility Criteria for the Clinical Data Management Job:

The ideal candidate will possess relevant clinical research experience along with the following qualifications:

  • Bachelor’s degree in a relevant field, such as Healthcare.
  • Basic knowledge of clinical data management within the pharmaceutical or biotechnology industry.
  • Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar).
  • Strong attention to detail and the ability to work effectively in a fast-paced environment.
  • Excellent communication skills and the ability to collaborate with cross-functional teams.
  • Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.

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